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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Reverse micellar microextraction for rapid analysis of thiol-containing peptides and amino acids by atmospheric-pressure matrix-assisted laser desorption/ionization ion trap and matrix-assisted laser desorption/ionization time-of-flight mass spectrom
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Reverse micellar microextraction for rapid analysis of thiol-containing peptides and amino acids by atmospheric-pressure matrix-assisted laser desorption/ionization ion trap and matrix-assisted laser desorption/ionization time-of-flight mass spectrom

机译:反向胶束微萃取通过大气压基质辅助激光解吸/电离离子阱和基质辅助激光解吸/电离飞行时间质谱快速分析含硫醇的肽和氨基酸

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摘要

Simple, rapid and inexpensive one-step reverse micellar microextraction (RMME) procedures were combined with matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS) for the determination of thiol-containing peptides and amino acids. In this investigation, a thiol-containing peptide (HW6) was chosen as model compound to understand the mechanism of RMME. The electrostatic interactions between the thiol-containing peptide and reverse micelles were proposed to be reason for the transfer of analytes from the aqueous phase to the organic phase. Reverse micelles were formed by the cationic surfactant, methyltrioctylammonium chloride (MTOAC). The best extraction efficiency of HW6 was obtained under the following conditions: pH 11.0, ionic strength 5.0 mM of KCl and micelle concentration 7.0 mM of MTOAC. The limits of detection (LODs) obtained for HW6 in water, urine and plasma samples were 0.15, 0.19 and 0.28 mu M, respectively, with relative standard deviation (RSD) values in the range +/- 8.8-10.5%. The sensitivity obtained in water by the present method was 45-fold higher than that of the conventional use of atmospheric-pressure (AP)-MALDI MS. Furthermore, the applicability of the proposed approach was extended for the determination of thiol-containing amino acids in sample solutions by using MALDI time-of-flight (TOF) MS. Copyright (c) 2008 John Wiley & Sons, Ltd.
机译:简单,快速,廉价的一步式反胶束微萃取(RMME)程序与基质辅助激光解吸/电离质谱(MALDI MS)结合使用,可测定含硫醇的肽和氨基酸。在这项研究中,选择含巯基的肽(HW6)作为模型化合物,以了解RMME的机理。提出了含硫醇的肽和反胶束之间的静电相互作用是将分析物从水相转移到有机相的原因。阳离子表面活性剂甲基三辛基氯化铵(MTOAC)形成反胶束。在以下条件下获得最佳的HW6提取效率:pH 11.0,离子强度5.0 mM的KCl和胶束浓度7.0 mM的MTOAC。水,尿液和血浆样品中HW6的检出限(LOD)分别为0.15、0.19和0.28μM,相对标准偏差(RSD)值在+/- 8.8-10.5%范围内。通过本方法在水中获得的灵敏度比常规使用的大气压(AP)-MALDI MS高45倍。此外,通过使用MALDI飞行时间(TOF)MS,所提出方法的适用性扩展到了样品溶液中含硫醇氨基酸的测定。版权所有(c)2008 John Wiley&Sons,Ltd.

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